RBM18

gene
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Also known as MGC2734

Summary

RBM18 (RNA binding motif protein 18, HGNC:28413) is a protein-coding gene on chromosome 9q33.2, encoding Probable RNA-binding protein 18 (Q96H35). It is a selective cancer dependency (DepMap: 15.2% of cell lines).

Predicted to enable RNA binding activity. Located in cytosol; intercellular bridge; and nucleoplasm.

Source: NCBI Gene 92400 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 27 total
  • Cancer dependency (DepMap): dependent in 15.2% of screened cell lines
  • MANE Select transcript: NM_033117

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:28413
Approved symbolRBM18
NameRNA binding motif protein 18
Location9q33.2
Locus typegene with protein product
StatusApproved
AliasesMGC2734
Ensembl geneENSG00000119446
Ensembl biotypeprotein_coding
Entrez92400

Gene structure

Transcript identifiers

Ensembl transcripts: 11 — 9 protein_coding, 2 protein_coding_CDS_not_defined

ENST00000417201, ENST00000483428, ENST00000491850, ENST00000870815, ENST00000870816, ENST00000870817, ENST00000870818, ENST00000870819, ENST00000870820, ENST00000919715, ENST00000919718

RefSeq mRNA: 1 — MANE Select: NM_033117 NM_033117

CCDS: CCDS6839

Canonical transcript exons

ENST00000417201 — 6 exons

ExonStartEnd
ENSE00001695302122264715122264840
ENSE00001945206122237622122242043
ENSE00003655163122261380122261508
ENSE00003662821122245256122245341
ENSE00003676218122251847122251973
ENSE00003687045122247518122247604

Expression profiles

Bgee: expression breadth ubiquitous, 251 present calls, max score 96.79.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 30.2623 / max 109.1478, expressed in 1819 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
10239028.58151819
1023891.1785808
1023880.5023263

Top tissues by expression

254 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
oocyteCL:000002396.79gold quality
tibialis anteriorUBERON:000138596.22gold quality
secondary oocyteCL:000065595.47gold quality
left ventricle myocardiumUBERON:000656694.65gold quality
deltoidUBERON:000147694.44gold quality
heart right ventricleUBERON:000208093.54gold quality
quadriceps femorisUBERON:000137793.41gold quality
vastus lateralisUBERON:000137993.33gold quality
myocardiumUBERON:000234993.24gold quality
biceps brachiiUBERON:000150793.20gold quality
cardiac muscle of right atriumUBERON:000337993.02gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451192.20gold quality
skeletal muscle tissue of biceps brachiiUBERON:000450291.58gold quality
skeletal muscle tissueUBERON:000113491.44gold quality
muscle tissueUBERON:000238591.21gold quality
ganglionic eminenceUBERON:000402390.84gold quality
cortical plateUBERON:000534390.64gold quality
ileal mucosaUBERON:000033189.47gold quality
hindlimb stylopod muscleUBERON:000425289.47gold quality
muscle of legUBERON:000138389.28gold quality
gastrocnemiusUBERON:000138889.10gold quality
islet of LangerhansUBERON:000000688.59gold quality
endothelial cellCL:000011588.29silver quality
stromal cell of endometriumCL:000225587.81gold quality
cardiac ventricleUBERON:000208286.44gold quality
heart left ventricleUBERON:000208486.43gold quality
smooth muscle tissueUBERON:000113586.32gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099186.20gold quality
prefrontal cortexUBERON:000045186.16gold quality
ventricular zoneUBERON:000305386.05gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes6.04

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

182 targeting RBM18, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-5692A100.0074.406850
HSA-MIR-3163100.0077.238605
HSA-MIR-4692100.0067.322066
HSA-MIR-450A-1-3P100.0069.331837
HSA-MIR-518D-5P100.0067.51979
HSA-MIR-518E-5P100.0067.66954
HSA-MIR-518F-5P100.0067.51979
HSA-MIR-519A-5P100.0067.66954
HSA-MIR-519B-5P100.0067.66954
HSA-MIR-519C-5P100.0067.66954
HSA-MIR-520C-5P100.0067.51979
HSA-MIR-522-5P100.0067.66954
HSA-MIR-523-5P100.0067.66954
HSA-MIR-526A-5P100.0067.51979
HSA-MIR-5011-5P100.0083.465820
HSA-MIR-5692B100.0071.322622
HSA-MIR-5692C100.0071.322622
HSA-MIR-366299.9973.825684
HSA-MIR-451499.9967.101870
HSA-MIR-196A-1-3P99.9972.152772
HSA-MIR-520G-5P99.9966.76658
HSA-MIR-548C-3P99.9974.017587
HSA-MIR-548N99.9871.944170
HSA-MIR-477599.9875.006394
HSA-MIR-520D-5P99.9873.344883
HSA-MIR-524-5P99.9873.434882
HSA-MIR-60799.9773.625593
HSA-MIR-50799.9770.111915
HSA-MIR-590-3P99.9674.346478
HSA-MIR-365899.9673.874379

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 15.2% of screened cell lines.

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriorbm18ENSDARG00000044255
mus_musculusRbm18ENSMUSG00000026889
rattus_norvegicusRbm18ENSRNOG00000006763
drosophila_melanogasterCG14414FBGN0030571

Protein

Protein identifiers

Probable RNA-binding protein 18Q96H35 (reviewed: Q96H35)

Alternative names: RNA-binding motif protein 18

All UniProt accessions (1): Q96H35

RefSeq proteins (1): NP_149108* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR000504RRM_domDomain
IPR012677Nucleotide-bd_a/b_plait_sfHomologous_superfamily
IPR035979RBD_domain_sfHomologous_superfamily
IPR039157RBM18_RRMDomain

Pfam: PF00076

UniProt features (3 total): chain 1, domain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96H35-F174.440.41

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 116 (showing top): GRAESSMANN_APOPTOSIS_BY_DOXORUBICIN_DN, GRAESSMANN_RESPONSE_TO_MC_AND_DOXORUBICIN_DN, CREB_Q2_01, ATF4_Q2, CREBP1CJUN_01, CREB_01, CGTSACG_PAX3_B, TGACGTCA_ATF3_Q6, NUYTTEN_NIPP1_TARGETS_DN, CCGNMNNTNACG_UNKNOWN, BRUINS_UVC_RESPONSE_VIA_TP53_GROUP_A, LINDGREN_BLADDER_CANCER_CLUSTER_1_UP, GOBERT_OLIGODENDROCYTE_DIFFERENTIATION_DN, BYSTRYKH_HEMATOPOIESIS_STEM_CELL_QTL_TRANS, STAT6_01

GO Biological Process (0):

GO Molecular Function (2): RNA binding (GO:0003723), nucleic acid binding (GO:0003676)

GO Cellular Component (3): nucleoplasm (GO:0005654), cytosol (GO:0005829), intercellular bridge (GO:0045171)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular anatomical structure3
nucleic acid binding1
binding1
nuclear lumen1
cytoplasm1

Protein interactions and networks

STRING

612 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
RBM18FAM32AQ9Y421541
RBM18SYF2O95926453
RBM18RNF151Q2KHN1451
RBM18UBOX5O94941450
RBM18SUPT7LO94864447
RBM18SYDE2Q5VT97440
RBM18CFAP97Q9P2B7440
RBM18GTF3C5Q9Y5Q8424
RBM18CMTR1Q8N1G2420
RBM18DCTN3O75935418
RBM18ZMAT2Q96NC0415
RBM18CRIPTQ9P021401
RBM18BEX5Q5H9J7397
RBM18PPP1R7Q15435389
RBM18OST4P0C6T2386

IntAct

9 interactions, top by confidence:

ABTypeScore
EPHA3RBM18psi-mi:“MI:0915”(physical association)0.370
RBM18NDUFAB1psi-mi:“MI:0915”(physical association)0.370
TAP2RBM18psi-mi:“MI:0915”(physical association)0.370
GCNT3RBM18psi-mi:“MI:0915”(physical association)0.370
RBM18CLTRNpsi-mi:“MI:0915”(physical association)0.370
RBM18GSNpsi-mi:“MI:0914”(association)0.350
RBM18SYT1psi-mi:“MI:0914”(association)0.350

BioGRID (28): ACTA2 (Affinity Capture-MS), GSN (Affinity Capture-MS), TMOD2 (Affinity Capture-MS), UBR3 (Affinity Capture-MS), MINA (Affinity Capture-MS), CAPZA2 (Affinity Capture-MS), CNRIP1 (Affinity Capture-MS), MINA (Affinity Capture-MS), TMOD2 (Affinity Capture-MS), GSN (Affinity Capture-MS), CNRIP1 (Affinity Capture-MS), UBR3 (Affinity Capture-MS), ACTA2 (Affinity Capture-MS), RBM18 (Negative Genetic), GSN (Affinity Capture-MS)

ESM2 similar proteins: A2VDZ9, A4IGK3, A5GFS8, B2GV05, G3V9R8, O22969, O77768, O95232, O95292, P07910, P11031, P52756, P53999, P57060, Q08DJ0, Q0IIC4, Q1RMU5, Q24K03, Q32KT0, Q3SX41, Q3ZCC5, Q4R947, Q5R601, Q5R6D0, Q5R6W3, Q5R8W6, Q5RA82, Q5RAM8, Q5SUF2, Q5ZIA0, Q5ZK63, Q63396, Q642H2, Q6PH81, Q86SE5, Q8BTF8, Q91YE7, Q96H35, Q96JC9, Q99J36

Diamond homologs: A6NFN3, B0XS28, B5DF91, O43347, O60176, O94432, O95758, P17225, P23246, P26599, P28644, P30352, P32831, P48809, P60047, P60048, P60049, P60050, P70372, Q00438, Q01130, Q04047, Q04836, Q06A98, Q06AT9, Q07955, Q09511, Q0VCY7, Q13242, Q15233, Q1JPY8, Q1LZD9, Q24491, Q28IQ9, Q29099, Q3MHR5, Q3MHX3, Q3YLA6, Q3ZCC5, Q4KLH4

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

27 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance19
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1075 predictions. Top by Δscore:

VariantEffectΔscore
9:122242042:CA:Cacceptor_gain1.0000
9:122242044:C:CCacceptor_gain1.0000
9:122245250:TCTTA:Tdonor_loss1.0000
9:122245251:CTTA:Cdonor_loss1.0000
9:122245252:TTAC:Tdonor_loss1.0000
9:122245253:TA:Tdonor_loss1.0000
9:122245254:ACCTT:Adonor_loss1.0000
9:122245255:C:CGdonor_loss1.0000
9:122245337:TATCT:Tacceptor_gain1.0000
9:122245339:TCTCT:Tacceptor_loss1.0000
9:122245340:CT:Cacceptor_gain1.0000
9:122245341:TCTGA:Tacceptor_loss1.0000
9:122245342:C:CCacceptor_gain1.0000
9:122245342:CTG:Cacceptor_loss1.0000
9:122245343:T:Aacceptor_loss1.0000
9:122247513:CGTA:Cdonor_loss1.0000
9:122247514:GTAC:Gdonor_loss1.0000
9:122247515:TAC:Tdonor_loss1.0000
9:122247516:ACCTT:Adonor_loss1.0000
9:122247517:CCT:Cdonor_gain1.0000
9:122247601:CTTC:Cacceptor_gain1.0000
9:122247603:TC:Tacceptor_gain1.0000
9:122247604:CC:Cacceptor_gain1.0000
9:122247605:C:CCacceptor_gain1.0000
9:122247606:T:Cacceptor_loss1.0000
9:122247610:C:CTacceptor_gain1.0000
9:122247610:C:Tacceptor_gain1.0000
9:122247611:A:Tacceptor_gain1.0000
9:122251970:GTATC:Gacceptor_loss1.0000
9:122251971:TATCT:Tacceptor_loss1.0000

AlphaMissense

1234 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
9:122242008:A:GL150P1.000
9:122242010:T:AK149N1.000
9:122242010:T:GK149N1.000
9:122242015:C:GA148P1.000
9:122242020:A:TI146N1.000
9:122242024:C:GA145P1.000
9:122247540:C:GR102P1.000
9:122247543:A:TV101E1.000
9:122247549:A:GL99P1.000
9:122247564:G:TA94D1.000
9:122247579:A:GL89P1.000
9:122247591:G:TA85D1.000
9:122247592:C:GA85P1.000
9:122247601:C:GA82P1.000
9:122251860:A:GF76S1.000
9:122251866:A:TV74D1.000
9:122251868:A:CF73L1.000
9:122251868:A:TF73L1.000
9:122251869:A:CF73C1.000
9:122251869:A:GF73S1.000
9:122251870:A:CF73V1.000
9:122251870:A:GF73L1.000
9:122251870:A:TF73I1.000
9:122251871:A:CC72W1.000
9:122251872:C:TC72Y1.000
9:122251873:A:GC72R1.000
9:122251876:A:GY71H1.000
9:122251878:C:AG70V1.000
9:122251878:C:TG70D1.000
9:122251879:C:GG70R1.000

dbSNP variants (sampled 300 via entrez): RS1000046070 (9:122244144 A>T), RS1000177950 (9:122253005 C>A,T), RS1000287105 (9:122257114 C>T), RS1000350388 (9:122264147 T>C), RS1000425441 (9:122263860 T>C), RS1000469272 (9:122257245 C>A), RS1000513900 (9:122255817 G>A,C), RS1000573854 (9:122257240 C>G), RS1000583539 (9:122255857 A>G), RS1000684752 (9:122262528 G>A), RS1000756767 (9:122262234 T>C), RS1001044238 (9:122238324 G>A), RS1001172832 (9:122258585 A>G), RS1001217233 (9:122262109 T>C), RS1001287127 (9:122258337 C>T)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

38 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Air Pollutantsaffects expression, increases abundance, decreases expression2
Valproic Aciddecreases expression, decreases methylation, increases expression2
dicrotophosdecreases expression1
methylmercuric chloridedecreases expression1
triphenyl phosphateaffects expression1
trichostatin Adecreases expression1
sodium arseniteaffects cotreatment, increases abundance, increases expression1
manganese chlorideincreases abundance, increases expression, affects cotreatment1
beta-methylcholineaffects expression1
cylindrospermopsinincreases expression1
CGP 52608affects binding, increases reaction1
ICG 001increases expression1
(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II)increases expression1
jinfukangdecreases expression1
Arsenicaffects cotreatment, increases abundance, increases expression1
Atrazineincreases expression1
Benzo(a)pyrenedecreases methylation1
Cisplatinincreases expression1
Copperdecreases expression, affects binding1
Demecolcineincreases expression1
Disulfiramaffects binding, decreases expression1
Doxorubicindecreases expression1
Ethyl Methanesulfonateincreases expression1
Formaldehydeincreases expression1
Hydrogen Peroxideaffects expression1
Manganeseincreases abundance, increases expression, affects cotreatment1
Methyl Methanesulfonateincreases expression1
Ozoneincreases abundance, affects expression1
Phenobarbitalaffects expression1
Smokedecreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.